Low-dose statin treatment increases prostate cancer aggressiveness

Prostate cancer is diagnosed late in life, when co-morbidities are frequent. Among them, hypertension, hypercholesterolemia, diabetes or metabolic syndrome exhibit an elevated incidence. In turn, prostate cancer patients frequently undergo chronic pharmacological treatments that could alter disease...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Oncotarget 2018-01, Vol.9 (2), p.1494-1504
Hauptverfasser: Caro-Maldonado, Alfredo, Camacho, Laura, Zabala-Letona, Amaia, Torrano, Verónica, Fernández-Ruiz, Sonia, Zamacola-Bascaran, Kepa, Arreal, Leire, Valcárcel-Jiménez, Lorea, Martín-Martín, Natalia, Flores, Juana M, Cortazar, Ana R, Zúñiga-García, Patricia, Arruabarrena-Aristorena, Amaia, Guillaumond, Fabienne, Cabrera, Diana, Falcón-Perez, Juan M, Aransay, Ana M, Gomez-Muñoz, Antonio, Olivan, Mireia, Morote, Juan, Carracedo, Arkaitz
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1504
container_issue 2
container_start_page 1494
container_title Oncotarget
container_volume 9
creator Caro-Maldonado, Alfredo
Camacho, Laura
Zabala-Letona, Amaia
Torrano, Verónica
Fernández-Ruiz, Sonia
Zamacola-Bascaran, Kepa
Arreal, Leire
Valcárcel-Jiménez, Lorea
Martín-Martín, Natalia
Flores, Juana M
Cortazar, Ana R
Zúñiga-García, Patricia
Arruabarrena-Aristorena, Amaia
Guillaumond, Fabienne
Cabrera, Diana
Falcón-Perez, Juan M
Aransay, Ana M
Gomez-Muñoz, Antonio
Olivan, Mireia
Morote, Juan
Carracedo, Arkaitz
description Prostate cancer is diagnosed late in life, when co-morbidities are frequent. Among them, hypertension, hypercholesterolemia, diabetes or metabolic syndrome exhibit an elevated incidence. In turn, prostate cancer patients frequently undergo chronic pharmacological treatments that could alter disease initiation, progression and therapy response. Here we show that treatment with anti-cholesterolemic drugs, statins, at doses achieved in patients, enhance the pro-tumorigenic activity of obesogenic diets. In addition, the use of a mouse model of prostate cancer and human prostate cancer xenografts revealed that simvastatin administration alone increases prostate cancer aggressiveness. cell line systems supported the notion that this phenomenon occurs, at least in part, through the direct action on cancer cells of low doses of statins, in range of what is observed in human plasma. In sum, our results reveal a prostate cancer experimental system where statins exhibit an undesirable effect, and warrant further research to address the relevance and implications of this observation in human prostate cancer.
doi_str_mv 10.18632/oncotarget.22217
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5788577</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1999677600</sourcerecordid><originalsourceid>FETCH-LOGICAL-c433t-4132630dacc186f68bf953806aa9390cf3f61944bd23b607ce6b9cf0aa26e72a3</originalsourceid><addsrcrecordid>eNpdUctOwzAQtBCIVqUfwAXlCIcUPxI7viCVCihSJS5wthxn0wa1cbHdIv4e90Ep-LIr78zs2IPQJcEDUnBGb21rbNBuCmFAKSXiBHWJzGRK85ydHvUd1Pf-HceTZ6Kg8hx1qMwIF1h20f3EfqaV9ZD4oEPTJsGBDgtoQ9K0JvYefLJ0djOFxOjWgEv0dOrA-2YNbSwX6KzWcw_9fe2ht8eH19E4nbw8PY-Gk9RkjIU0I4xyhittTPRf86KsZc4KzLWWTGJTs5pHz1lZUVZyLAzwUpoaa005CKpZD93tdJercgGViR6dnqulaxbafSmrG_V30jYzNbVrlYuiyIWIAjc7gdk_2ng4UZs7TEnG8qJYk4i93i9z9mMFPqhF4w3M57oFu_KKSCm5EBzjCCU7qInf5B3UB22C1TYq9RuV2kYVOVfHbzkwfoJh35qHk0A</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1999677600</pqid></control><display><type>article</type><title>Low-dose statin treatment increases prostate cancer aggressiveness</title><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Free E- Journals</source><source>PubMed Central Open Access</source><creator>Caro-Maldonado, Alfredo ; Camacho, Laura ; Zabala-Letona, Amaia ; Torrano, Verónica ; Fernández-Ruiz, Sonia ; Zamacola-Bascaran, Kepa ; Arreal, Leire ; Valcárcel-Jiménez, Lorea ; Martín-Martín, Natalia ; Flores, Juana M ; Cortazar, Ana R ; Zúñiga-García, Patricia ; Arruabarrena-Aristorena, Amaia ; Guillaumond, Fabienne ; Cabrera, Diana ; Falcón-Perez, Juan M ; Aransay, Ana M ; Gomez-Muñoz, Antonio ; Olivan, Mireia ; Morote, Juan ; Carracedo, Arkaitz</creator><creatorcontrib>Caro-Maldonado, Alfredo ; Camacho, Laura ; Zabala-Letona, Amaia ; Torrano, Verónica ; Fernández-Ruiz, Sonia ; Zamacola-Bascaran, Kepa ; Arreal, Leire ; Valcárcel-Jiménez, Lorea ; Martín-Martín, Natalia ; Flores, Juana M ; Cortazar, Ana R ; Zúñiga-García, Patricia ; Arruabarrena-Aristorena, Amaia ; Guillaumond, Fabienne ; Cabrera, Diana ; Falcón-Perez, Juan M ; Aransay, Ana M ; Gomez-Muñoz, Antonio ; Olivan, Mireia ; Morote, Juan ; Carracedo, Arkaitz</creatorcontrib><description>Prostate cancer is diagnosed late in life, when co-morbidities are frequent. Among them, hypertension, hypercholesterolemia, diabetes or metabolic syndrome exhibit an elevated incidence. In turn, prostate cancer patients frequently undergo chronic pharmacological treatments that could alter disease initiation, progression and therapy response. Here we show that treatment with anti-cholesterolemic drugs, statins, at doses achieved in patients, enhance the pro-tumorigenic activity of obesogenic diets. In addition, the use of a mouse model of prostate cancer and human prostate cancer xenografts revealed that simvastatin administration alone increases prostate cancer aggressiveness. cell line systems supported the notion that this phenomenon occurs, at least in part, through the direct action on cancer cells of low doses of statins, in range of what is observed in human plasma. In sum, our results reveal a prostate cancer experimental system where statins exhibit an undesirable effect, and warrant further research to address the relevance and implications of this observation in human prostate cancer.</description><identifier>ISSN: 1949-2553</identifier><identifier>EISSN: 1949-2553</identifier><identifier>DOI: 10.18632/oncotarget.22217</identifier><identifier>PMID: 29416709</identifier><language>eng</language><publisher>United States: Impact journals</publisher><subject>Life Sciences ; Priority Research Paper</subject><ispartof>Oncotarget, 2018-01, Vol.9 (2), p.1494-1504</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright: © 2018 Caro-Maldonado et al. 2018</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c433t-4132630dacc186f68bf953806aa9390cf3f61944bd23b607ce6b9cf0aa26e72a3</citedby><cites>FETCH-LOGICAL-c433t-4132630dacc186f68bf953806aa9390cf3f61944bd23b607ce6b9cf0aa26e72a3</cites><orcidid>0000-0001-7456-7315</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788577/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788577/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29416709$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://amu.hal.science/hal-02143588$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Caro-Maldonado, Alfredo</creatorcontrib><creatorcontrib>Camacho, Laura</creatorcontrib><creatorcontrib>Zabala-Letona, Amaia</creatorcontrib><creatorcontrib>Torrano, Verónica</creatorcontrib><creatorcontrib>Fernández-Ruiz, Sonia</creatorcontrib><creatorcontrib>Zamacola-Bascaran, Kepa</creatorcontrib><creatorcontrib>Arreal, Leire</creatorcontrib><creatorcontrib>Valcárcel-Jiménez, Lorea</creatorcontrib><creatorcontrib>Martín-Martín, Natalia</creatorcontrib><creatorcontrib>Flores, Juana M</creatorcontrib><creatorcontrib>Cortazar, Ana R</creatorcontrib><creatorcontrib>Zúñiga-García, Patricia</creatorcontrib><creatorcontrib>Arruabarrena-Aristorena, Amaia</creatorcontrib><creatorcontrib>Guillaumond, Fabienne</creatorcontrib><creatorcontrib>Cabrera, Diana</creatorcontrib><creatorcontrib>Falcón-Perez, Juan M</creatorcontrib><creatorcontrib>Aransay, Ana M</creatorcontrib><creatorcontrib>Gomez-Muñoz, Antonio</creatorcontrib><creatorcontrib>Olivan, Mireia</creatorcontrib><creatorcontrib>Morote, Juan</creatorcontrib><creatorcontrib>Carracedo, Arkaitz</creatorcontrib><title>Low-dose statin treatment increases prostate cancer aggressiveness</title><title>Oncotarget</title><addtitle>Oncotarget</addtitle><description>Prostate cancer is diagnosed late in life, when co-morbidities are frequent. Among them, hypertension, hypercholesterolemia, diabetes or metabolic syndrome exhibit an elevated incidence. In turn, prostate cancer patients frequently undergo chronic pharmacological treatments that could alter disease initiation, progression and therapy response. Here we show that treatment with anti-cholesterolemic drugs, statins, at doses achieved in patients, enhance the pro-tumorigenic activity of obesogenic diets. In addition, the use of a mouse model of prostate cancer and human prostate cancer xenografts revealed that simvastatin administration alone increases prostate cancer aggressiveness. cell line systems supported the notion that this phenomenon occurs, at least in part, through the direct action on cancer cells of low doses of statins, in range of what is observed in human plasma. In sum, our results reveal a prostate cancer experimental system where statins exhibit an undesirable effect, and warrant further research to address the relevance and implications of this observation in human prostate cancer.</description><subject>Life Sciences</subject><subject>Priority Research Paper</subject><issn>1949-2553</issn><issn>1949-2553</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpdUctOwzAQtBCIVqUfwAXlCIcUPxI7viCVCihSJS5wthxn0wa1cbHdIv4e90Ep-LIr78zs2IPQJcEDUnBGb21rbNBuCmFAKSXiBHWJzGRK85ydHvUd1Pf-HceTZ6Kg8hx1qMwIF1h20f3EfqaV9ZD4oEPTJsGBDgtoQ9K0JvYefLJ0djOFxOjWgEv0dOrA-2YNbSwX6KzWcw_9fe2ht8eH19E4nbw8PY-Gk9RkjIU0I4xyhittTPRf86KsZc4KzLWWTGJTs5pHz1lZUVZyLAzwUpoaa005CKpZD93tdJercgGViR6dnqulaxbafSmrG_V30jYzNbVrlYuiyIWIAjc7gdk_2ng4UZs7TEnG8qJYk4i93i9z9mMFPqhF4w3M57oFu_KKSCm5EBzjCCU7qInf5B3UB22C1TYq9RuV2kYVOVfHbzkwfoJh35qHk0A</recordid><startdate>20180105</startdate><enddate>20180105</enddate><creator>Caro-Maldonado, Alfredo</creator><creator>Camacho, Laura</creator><creator>Zabala-Letona, Amaia</creator><creator>Torrano, Verónica</creator><creator>Fernández-Ruiz, Sonia</creator><creator>Zamacola-Bascaran, Kepa</creator><creator>Arreal, Leire</creator><creator>Valcárcel-Jiménez, Lorea</creator><creator>Martín-Martín, Natalia</creator><creator>Flores, Juana M</creator><creator>Cortazar, Ana R</creator><creator>Zúñiga-García, Patricia</creator><creator>Arruabarrena-Aristorena, Amaia</creator><creator>Guillaumond, Fabienne</creator><creator>Cabrera, Diana</creator><creator>Falcón-Perez, Juan M</creator><creator>Aransay, Ana M</creator><creator>Gomez-Muñoz, Antonio</creator><creator>Olivan, Mireia</creator><creator>Morote, Juan</creator><creator>Carracedo, Arkaitz</creator><general>Impact journals</general><general>Impact Journals LLC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7456-7315</orcidid></search><sort><creationdate>20180105</creationdate><title>Low-dose statin treatment increases prostate cancer aggressiveness</title><author>Caro-Maldonado, Alfredo ; Camacho, Laura ; Zabala-Letona, Amaia ; Torrano, Verónica ; Fernández-Ruiz, Sonia ; Zamacola-Bascaran, Kepa ; Arreal, Leire ; Valcárcel-Jiménez, Lorea ; Martín-Martín, Natalia ; Flores, Juana M ; Cortazar, Ana R ; Zúñiga-García, Patricia ; Arruabarrena-Aristorena, Amaia ; Guillaumond, Fabienne ; Cabrera, Diana ; Falcón-Perez, Juan M ; Aransay, Ana M ; Gomez-Muñoz, Antonio ; Olivan, Mireia ; Morote, Juan ; Carracedo, Arkaitz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c433t-4132630dacc186f68bf953806aa9390cf3f61944bd23b607ce6b9cf0aa26e72a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Life Sciences</topic><topic>Priority Research Paper</topic><toplevel>online_resources</toplevel><creatorcontrib>Caro-Maldonado, Alfredo</creatorcontrib><creatorcontrib>Camacho, Laura</creatorcontrib><creatorcontrib>Zabala-Letona, Amaia</creatorcontrib><creatorcontrib>Torrano, Verónica</creatorcontrib><creatorcontrib>Fernández-Ruiz, Sonia</creatorcontrib><creatorcontrib>Zamacola-Bascaran, Kepa</creatorcontrib><creatorcontrib>Arreal, Leire</creatorcontrib><creatorcontrib>Valcárcel-Jiménez, Lorea</creatorcontrib><creatorcontrib>Martín-Martín, Natalia</creatorcontrib><creatorcontrib>Flores, Juana M</creatorcontrib><creatorcontrib>Cortazar, Ana R</creatorcontrib><creatorcontrib>Zúñiga-García, Patricia</creatorcontrib><creatorcontrib>Arruabarrena-Aristorena, Amaia</creatorcontrib><creatorcontrib>Guillaumond, Fabienne</creatorcontrib><creatorcontrib>Cabrera, Diana</creatorcontrib><creatorcontrib>Falcón-Perez, Juan M</creatorcontrib><creatorcontrib>Aransay, Ana M</creatorcontrib><creatorcontrib>Gomez-Muñoz, Antonio</creatorcontrib><creatorcontrib>Olivan, Mireia</creatorcontrib><creatorcontrib>Morote, Juan</creatorcontrib><creatorcontrib>Carracedo, Arkaitz</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oncotarget</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Caro-Maldonado, Alfredo</au><au>Camacho, Laura</au><au>Zabala-Letona, Amaia</au><au>Torrano, Verónica</au><au>Fernández-Ruiz, Sonia</au><au>Zamacola-Bascaran, Kepa</au><au>Arreal, Leire</au><au>Valcárcel-Jiménez, Lorea</au><au>Martín-Martín, Natalia</au><au>Flores, Juana M</au><au>Cortazar, Ana R</au><au>Zúñiga-García, Patricia</au><au>Arruabarrena-Aristorena, Amaia</au><au>Guillaumond, Fabienne</au><au>Cabrera, Diana</au><au>Falcón-Perez, Juan M</au><au>Aransay, Ana M</au><au>Gomez-Muñoz, Antonio</au><au>Olivan, Mireia</au><au>Morote, Juan</au><au>Carracedo, Arkaitz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Low-dose statin treatment increases prostate cancer aggressiveness</atitle><jtitle>Oncotarget</jtitle><addtitle>Oncotarget</addtitle><date>2018-01-05</date><risdate>2018</risdate><volume>9</volume><issue>2</issue><spage>1494</spage><epage>1504</epage><pages>1494-1504</pages><issn>1949-2553</issn><eissn>1949-2553</eissn><abstract>Prostate cancer is diagnosed late in life, when co-morbidities are frequent. Among them, hypertension, hypercholesterolemia, diabetes or metabolic syndrome exhibit an elevated incidence. In turn, prostate cancer patients frequently undergo chronic pharmacological treatments that could alter disease initiation, progression and therapy response. Here we show that treatment with anti-cholesterolemic drugs, statins, at doses achieved in patients, enhance the pro-tumorigenic activity of obesogenic diets. In addition, the use of a mouse model of prostate cancer and human prostate cancer xenografts revealed that simvastatin administration alone increases prostate cancer aggressiveness. cell line systems supported the notion that this phenomenon occurs, at least in part, through the direct action on cancer cells of low doses of statins, in range of what is observed in human plasma. In sum, our results reveal a prostate cancer experimental system where statins exhibit an undesirable effect, and warrant further research to address the relevance and implications of this observation in human prostate cancer.</abstract><cop>United States</cop><pub>Impact journals</pub><pmid>29416709</pmid><doi>10.18632/oncotarget.22217</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-7456-7315</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1949-2553
ispartof Oncotarget, 2018-01, Vol.9 (2), p.1494-1504
issn 1949-2553
1949-2553
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5788577
source EZB-FREE-00999 freely available EZB journals; PubMed Central; Free E- Journals; PubMed Central Open Access
subjects Life Sciences
Priority Research Paper
title Low-dose statin treatment increases prostate cancer aggressiveness
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T15%3A23%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Low-dose%20statin%20treatment%20increases%20prostate%20cancer%20aggressiveness&rft.jtitle=Oncotarget&rft.au=Caro-Maldonado,%20Alfredo&rft.date=2018-01-05&rft.volume=9&rft.issue=2&rft.spage=1494&rft.epage=1504&rft.pages=1494-1504&rft.issn=1949-2553&rft.eissn=1949-2553&rft_id=info:doi/10.18632/oncotarget.22217&rft_dat=%3Cproquest_pubme%3E1999677600%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1999677600&rft_id=info:pmid/29416709&rfr_iscdi=true